- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Capillary Bed.
Displaying page 1 of 1.
EudraCT Number: 2013-002189-38 | Sponsor Protocol Number: 44945 | Start Date*: 2017-10-11 |
Sponsor Name:Erasmus Medical Center | ||
Full Title: OPTIMIZING PERIPHERAL CIRCULATION WITH VASODILATOR THERAPY IN CRITICALLY ILL PATIENTS WITH CIRCULATORY SHOCK: A PILOT STUDY | ||
Medical condition: Circulatory shock | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004972-20 | Sponsor Protocol Number: PST2744-DM-04-012 | Start Date*: 2007-01-18 | |||||||||||
Sponsor Name:Sigma-Tau i.f.r. S.p.A. | |||||||||||||
Full Title: A Phase II Study to assess the hemodynamic effects of ISTAROXIME, a novel lusinotropic agent, in patients hospitalized with worsening heart failure and a reduced left ventricular systolic function. | |||||||||||||
Medical condition: Chronic heart failure and left ventricular systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001020-38 | Sponsor Protocol Number: CRFB002EDE18 | Start Date*: 2011-06-24 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 6-month multicenter, randomized, double-masked phase IIIb-study comparing the efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal imp... | |||||||||||||
Medical condition: visual impairment due to macular edema following central retinal vein occlusion (CRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013929-42 | Sponsor Protocol Number: 39588146AHF2001 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Investigate the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of JNJ-39588146 in Subjects with Heart Failure | |||||||||||||
Medical condition: JNJ-39588146 is being developed for the treatment of heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001179-21 | Sponsor Protocol Number: 11-EI-0263 | Start Date*: 2018-01-17 |
Sponsor Name:The National Eye Institute | ||
Full Title: A Pilot Study for the Evaluation of Minocycline as a Microglia Inhibitor in the Treatment of Branch Retinal Vein Occlusions | ||
Medical condition: Branch Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001143-12 | Sponsor Protocol Number: 11-EI-0264 | Start Date*: 2018-01-09 |
Sponsor Name:The National Eye Institute | ||
Full Title: A Pilot Study for the Evaluation of Minocycline as a Microglia Inhibitor in the Treatment of Central Retinal Vein Occlusions | ||
Medical condition: Central Retinal Vein Occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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